Canonical Allele Identifier: CA500154547
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755345-G-A
MyVariant Identifiers: chr17:g.41832713G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755345G>A , CM000679.2:g.43755345G>A GRCh38
NC_000017.10:g.41832713G>A , CM000679.1:g.41832713G>A GRCh37
NC_000017.9:g.39188239G>A NCBI36
NG_008078.2:g.8444C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.639C>T MANE Select ENSP00000301691.1:p.Tyr213=
ENST00000301691.2:c.639C>T ENSP00000301691.1:p.Tyr213=
NM_025237.2:c.639C>T NP_079513.1:p.Tyr213=
NM_025237.3:c.639C>T MANE Select NP_079513.1:p.Tyr213=
Search 100 bp 5'
Search 100 bp 3'